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DHX15

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protein-coding gene in the species Homo sapiens

External resources

RefSeq RNA ID
NM_001358[೧]
XM_047449698[೨]
XM_047449699[೨]
Ensembl transcript ID
ENST00000513092[೩]
ENST00000336812[೩]
ENST00000503562[೩]
ENST00000504279[೩]
ENST00000508032[೩]
ENST00000508368[೩]
ENST00000510645[೩]
ENST00000511553[೩]
ENST00000512903[೩]
ENST00000513036[೩]
Entrez Gene ID
1665[೧]
UMLS CUI
C1413955[೪]
Ensembl gene ID
ENSG00000109606[೩]
OMIM ID
603403[೫]
HGNC ID
2738[೧]
HGNC gene symbol
DHX15[೧]
Freebase ಐಡಿ
/m/040853w

ಉದಾಹರಣೆಗೆ

ವಂಶವಾಹಿ[೩]

ಉಪವರ್ಗ

protein-coding gene[೬]

found in taxon

Homo sapiens[೩]

encodes

DEAH-box helicase 15[೭]

genetic association

myopia[೮]

determination method or standard: genome-wide association study, TAS

chromosome

human chromosome 4[೩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[೩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

24517441[೩]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 4

24519064[೩]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 4

genomic end

24586173[೩]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 4

24584554[೩]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 4

cytogenetic location

4p15.2[೧]

HomoloGene ID

1040[೧]

Gene Atlas image

ortholog

Dhx15[೯][೧೦]

found in taxon: house mouse

PRP43[೯]

found in taxon: Saccharomyces cerevisiae S288c

Dhx15[೯][೧೦]

found in taxon: brown rat

Dhx15[೯][೧೦]

found in taxon: Drosophila melanogaster

dhx15[೯]

found in taxon: Danio rerio

ddx-15[೯][೧೦]

found in taxon: Caenorhabditis elegans

expressed in

cartilage tissue[೧೧]

series ordinal: 1

tibia[೧೧]

series ordinal: 2

germinal epithelium[೧೧]

series ordinal: 3

mucosa of sigmoid colon[೧೧]

series ordinal: 4

visceral pleura[೧೧]

series ordinal: 5

skin of hip[೧೧]

series ordinal: 6

parietal pleura[೧೧]

series ordinal: 7

ಭ್ರೂಣ[೧೧]

series ordinal: 8

ventricular zone[೧೧]

series ordinal: 9

skin of thigh[೧೧]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/1665[೧೨]

Reference

  1. ↑ ೧.೦ ೧.೧ ೧.೨ ೧.೩ ೧.೪ ೧.೫ NCBI Gene, ೧೫ ಮೇ 2022, 1665
  2. ↑ ೨.೦ ೨.೧ NCBI Gene, ೧೦ ಏಪ್ರಿಲ್ 2022, 1665
  3. ↑ ೩.೦೦ ೩.೦೧ ೩.೦೨ ೩.೦೩ ೩.೦೪ ೩.೦೫ ೩.೦೬ ೩.೦೭ ೩.೦೮ ೩.೦೯ ೩.೧೦ ೩.೧೧ ೩.೧೨ ೩.೧೩ ೩.೧೪ ೩.೧೫ ೩.೧೬ ೩.೧೭ ೩.೧೮ ensembl Release 106, ENSG00000109606
  4. ↑ UMLS 2023, ೧೫ ಜೂನ್ 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, ೧೯ ಆಗಸ್ಟ್ 2019
  6. ↑ Ensembl Release 87, ENSG00000109606
  7. ↑ UniProt, ೬ ಜುಲೈ 2017, O43143
  8. ↑ Phenocarta, A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1665, http://www.genome.gov/gwastudies/index.cfm?gene=DHX15, ೨೫ ಮೇ 2020
  9. ↑ ೯.೦ ೯.೧ ೯.೨ ೯.೩ ೯.೪ ೯.೫ HomoloGene build68, 1040
  10. ↑ ೧೦.೦ ೧೦.೧ ೧೦.೨ ೧೦.೩ Orthologous MAtrix, https://omabrowser.org/oma/vps/O43143/
  11. ↑ ೧೧.೦೦ ೧೧.೦೧ ೧೧.೦೨ ೧೧.೦೩ ೧೧.೦೪ ೧೧.೦೫ ೧೧.೦೬ ೧೧.೦೭ ೧೧.೦೮ ೧೧.೦೯ Bgee, ೭ ಜೂನ್ 2024, https://www.bgee.org/gene/ENSG00000109606
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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